A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660309



Internal ID9926414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:96708579..96709335hg38UCSC Ensembl
Outerchr14:96708208..96709705hg38UCSC Ensembl
Innerchr14:97174916..97175672hg19UCSC Ensembl
Outerchr14:97174545..97176042hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg381498
hg191498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5484548, essv6407874, essv5479746, essv6532351, essv5410421
SamplesHG01521, HG01518, HG01519, HG01515, HG01516
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660309
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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